Optical chiral nematics

Chiral nematic Hquid crystals are sometimes referred to as spontaneously twisted nematics, and hence a special case of the nematic phase. The essential requirement for the chiral nematic stmcture is a chiral center that acts to bias the director of the Hquid crystal with a spontaneous cumulative twist. An ordinary nematic Hquid crystal can be converted into a chiral nematic by adding an optically active compound (4). In many cases the inverse of the pitch is directiy proportional to the molar concentration of the optically active compound. Racemic mixtures (1 1 mixtures of both isomers) of optically active mesogens form nematic rather than chiral nematic phases. Because of their twist encumbrance, chiral nematic Hquid crystals generally are more viscous than nematics (6). 

The polyamides are soluble in high strength sulfuric acid or in mixtures of hexamethylphosphoramide, /V, /V- dim ethyl acetam i de and LiCl. In the latter, compHcated relationships exist between solvent composition and the temperature at which the Hquid crystal phase forms. The polyamide solutions show an abmpt decrease in viscosity which is characteristic of mesophase formation when a critical volume fraction of polymer ( ) is exceeded. The viscosity may decrease, however, in the Hquid crystal phase if the molecular ordering allows the rod-shaped entities to gHde past one another more easily despite the higher concentration. The Hquid crystal phase is optically anisotropic and the texture is nematic. The nematic texture can be transformed to a chiral nematic texture by adding chiral species as a dopant or incorporating a chiral unit in the main chain as a copolymer (30). 

Liquid Crystalline Structures. In certain ceUular organeUes, deoxyribonucleic acid (DNA) occurs in a concentrated form. Striking similarities between the optical properties derived from the underlying supramolecular organization of the concentrated DNA phases and those observed in chiral nematic textures have been described (36). Concentrated aqueous solutions of nucleic acids exhibit a chiral nematic texture in vitro (29,37). 

To produce novel LC phase behavior and properties, a variety of polymer/LC composites have been developed. These include systems which employ liquid crystal polymers (5), phase separation of LC droplets in polymer dispersed liquid crystals (PDLCs) (4), incorporating both nematic (5,6) and ferroelectric liquid crystals (6-10). Polymer/LC gels have also been studied which are formed by the polymerization of small amounts of monomer solutes in a liquid crystalline solvent (11). The polymer/LC gel systems are of particular interest, rendering bistable chiral nematic devices (12) and polymer stabilized ferroelectric liquid crystals (PSFLCs) (1,13), which combine fast electro-optic response (14) with the increased mechanical stabilization imparted by the polymer (75). 

If the molecules of a liquid crystal are optically active Ichiral), then the nematic phase is not formed. Instead of the director being locally constant as is the case for nematics, the director rotates in helical fashion throughout the sample, Within any plane perpendicular to the helical axis the order is nematic-like. In other words, as in a nematic there is only orienlalional order in chiral nematic liquid crystals, and no positional order. 

The polyamides are soluble in high sirength sulfuric acid or in mixtures of hexamelhylphosphoiamide. AMV-diinethylaeciamidc. and l.ifT. The liquid-crystal phase is optically anisotropic and the texture is nematic. The nematic texture can he transformed lo a chiral nematic texture by adding chiral species us a dopant or incorporating a chiral unit in the main chain as a copolymer. 

A cholesteric, or chiral nematic (N ) phase. This is a positionally disordered fluid in which the constituent molecules align on average their axes along a common direction called the nematic director. Being the DNA helices chiral, the orientational order develops an additional macro-helical superstructure with the twist axis perpendicular to the local director. The phase thus consists of local nematic layers continuously twisted with respect to each other, with periodicity p/2 (where p is the cholesteric pitch see Fig. 8a) [27,28]. For 150-bp helices, the N phase appears at a concentration around 150 mg/mL in 100 mM monovalent salt conditions. This LC phase is easily observed in polarized optical microscopy. Since the N pitch extends to tens of micrometers (that is, across... 

H. Goto, K. Akagi, Optically Active Conjugated Polymers Prepared from Achiral Monomers by Polycondensation in a Chiral Nematic Solvent, Angetv. Chem. Int. Ed. 2005, 44, 4322-4328. 

A large number of azobenzene-based amorphous and liquid crystalline polymers, particularly polyacrylates and polymethacrylates with chiral azobenzene pendants, have been prepared for the development of data storage and photonic devices [1-3,11-14]. For instance, the introduction of optically active mesogenic azobenzene residues into the side groups of the polymers produces chiral nematic and cholesteric phases, which are regulated by photoisomerization of the azobenzene units [10,14]. In most cases, however, the optical activity and chiroptical... 

The major difference between the configuration of the OMI sandwich cell and other STN-LCDs is that the optical path difference (5 = And 1 pm) is much lower. There is no requirement for a significant pretilt (0 < 0 < 5°), the twist angle of the chiral nematic layer is lower (180°), the front polariser is parallel to the nematic director (a = 0°) and the polariser and analyser are crossed (P = 90°). The 180° twist gives rise to strong interference between the two elliptically polarised rays. If the optical path difference is small, e.g. 0.4 m, a bright, white, non-dispersive off-state is produced. The chiral nematic mixture should be of positive dielectric anisotropy, low birefringence and exhibit a low cell gap to pitch ratio dip 0.3). 

The electro-optical characteristics of multiplexed STN-LCDs exhibit a significant dependence on temperature. This has to be compensated in order to avoid variations of the optical performance of the display with temperatures. This can be achieved electronically. However, this problem can also be solved by the use of optically active, chiral dopants. The capacitive threshold voltage of a chiral nematic mixture depends on the pitch of the mixture ... 

The application of an electric field above the threshold value results in a reorientation of the nematic liquid crystal mixture, if the nematic phase is of negative dielectric anisotropy. The optically active dopant then applies a torque to the nematic phase and causes a helical structure to be formed in the plane of the display. The guest dye molecules are also reoriented and, therefore, the display appears coloured in the activated pixels. Thus, a positive contrast display is produced of coloured information against a white background. The threshold voltage is dependent upon the elastic constants, the magnitude of the dielectric anisotropy, and the ratio of the cell gap to the chiral nematic pitch ... 

Analysis of the electro-optical characteristics of GH-LCDs showed that for all types of guest-host chiral nematic phase change effects the contrast is greatest when... 

Cholesteric liquid crystals are optically active nematic phases as a result of their gradual twist in orientational alignment. Therefore, cholesteric liquid-crystalline solvents are expected to induce enantioselectivity in chemical reactions see reference [713] for a review on photoasymmetric induction by chiral mesophases. The existing results are not very promising. So far, the maximum photoasymmetric induction reported has... 

The material was chiral-nematic and had an apparent glass transition at 276 K and a clearing point at 325.2 K, as judged by DSC measurements. The clearing point was very sharp, the biphasic range being 0.5 K as determined by optical microscopy. 

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